The effects of Er3+ ion concentration on 2.0-μm emission performance in Ho3+/Tm3+ co-doped Na5Y9F32 single crystal under 800-nm excitation

Na₅Y₉F₃₂ single crystals doped with ~0.8-mol% Ho³⁺,~1-mol% Tm³⁺,and various Er³⁺ ion concentrations were prepared by a modified Bridgman method.The effects of Er³⁺ion concentration on 2.0-μm emission excited by an800-nm laser diode were investigated with the help of their spectroscopic properties.The intensity of 2.0-μm emission reached to maximum when the Er³⁺ ion concentration was ~1 mol%.The energy transfer mechanisms between Er³⁺,Ho³⁺,and Tm³⁺ ions were identified from the change of the absorption spectra,the emission spectra,and the measured decay curves.The maximum 2.0-μm emission cross section of the Er³⁺/Ho³⁺/Tm³⁺tri-doped Na₅Y₉F₃₂ single crystal reached 5.26 × 10^-21 cm².The gain cross section spectra were calculated according to the absorption and emission cross section spectra.The cross section for ~2.0-μm emission became a positive gain once the inversion level of population was reached 30%.The energy transfer efficiency was further increased by 11.81% through the incorporation of Er³⁺ ion into Ho³⁺/Tm³⁺ system estimated from the measured lifetimes of Ho³⁺/Tm³⁺-and Er³⁺/Ho³⁺/Tm³⁺-doped Na₅Y₉F₃₂single crystals.The present results illustrated that the Er³⁺/Ho³⁺/Tm³⁺tri-doped Na₅Y₉F₃₂ single crystals can be used as promising candidate for 2.0-μm laser.     

联吡啶催化的马来酸酐与环氧丙烷共聚物的结构分析

用联吡啶在室温下催化(MA)与环氧丙烷(PO)、环氧氯丙烷(ECH)开环交替共聚，用核磁共振技术研究了共聚物的交替度，测得共聚物中马来酸酐含量达48％以上。     

Br?nsted酸性离子液体活化电极催化制氢性能研究

分别采用玻碳( GC)、铂( Pt)和金( Au)电极研究了在Br?nsted酸性离子液体[ HMIm] HSO4中电解水制氢的催化活性,活性大小为Pt > Au >> GC。水中离子液体的含量对析氢电流影响很大,当[ HMIm] HSO4含量为30%(V/V)时,Pt电极催化电解水产氢的阈值电位高达-0.3 V (Ag丝为准参比电极, Ag QRE),在-0.5 V (Ag QRE)处电流密度高达110.52 mA/cm2,为相同条件下Au电极的15倍,GC电极的650倍。计算结果表明,Pt电极在该电解液中的反应活化能为5.68 kJ/mol。电极的高催化活性与[ HMIm] HSO4电离产生的质子有关,使水以H3 O+的形式捕集电子,效率更高。     

由2′,4′-二氢-6′-甲氧基-3′,5′-二甲基查耳酮合成新黄酮

在DMSO/I2的氧化作用下,由2′,4′-二氢-6′-甲氧基-3′,5′-二甲基查耳酮可合成一种全新结构的黄酮:7-羟基-5-甲氧基-6,8-二甲基黄酮(产率91%),而在HCl/MeOH作用下则得到了两种黄烷酮:7-羟基-5-甲氧基-6,8-二甲基黄烷酮(产率70%)和5,7-二羟基-6,8-二甲基黄烷酮(产率20%)。     

5-甲基色胺衍生物的合成

以5-甲基色胺盐酸盐和邻溴苯乙酸为例, 研究了5-甲基色胺衍生物的合成方法. 在室温下用二环己基碳二亚胺(DCC)作为脱水剂, N-羟基琥珀酰亚胺(NHS)活化酯法一锅法合成5-甲基色胺衍生物, 并通过FTIR、MS、1H NMR、13C NMR确定了目标化合物结构.     

分子模型及其在手性识别机理研究上的应用

介绍了近十几年来在色谱手性识别机理研究中的分子模型。在这些模型中,采用量子力学、分子力学和分子动力学等方法计算了手性选择试剂与对映体之间的相互作用,并借助X射线晶体学、核磁共振技术和计算机模拟等技术建立了各种分子模型,研究在手性化合物分离过程中的手性识别机理。     

一种新颖的短线阵高精度定位系统

本文提出了一种基于自适应相位差计的方位序列估计技术,在应用于一个短线阵的分裂波束定向系统时,不仅有较高的测向精度,而且因为可以获得较高的阵处理增益,因而能对远距离目标进行精确定位。